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Links from OMIM

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LHB
(I35T +1 more)
Single nucleotide variant
(missense variant)
LUTEINIZING HORMONE POLYMORPHISM
GBenign
MC4R
(I251fs)
Deletion
(frameshift variant)
Obesity
+3 more
GPathogenic/Likely pathogenic
IL1RN
Microsatellite
(intron variant)
Gastric cancer susceptibility after h. pylori infection
+1 more
GPathogenic; risk factor
LMNA
(R482Q +2 more)
Single nucleotide variant
(missense variant)
not provided
+15 more
GPathogenic
CAST, LOC101929710
+1 more
(G483R +1 more)
Single nucleotide variant
(missense variant)
Obesity due to prohormone convertase I deficiency
GPathogenic
GHR
Single nucleotide variant
(synonymous variant)
not provided
GPathogenic
PPARG
Single nucleotide variant
(synonymous variant +1 more)
Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension
+3 more
GBenign/Likely benign
PPARG
(P12A +2 more)
Single nucleotide variant
(missense variant +1 more)
Diabetes mellitus, noninsulin-dependent, modifier of
+3 more
Grisk factor
LOC110121472, TCF7L2
Single nucleotide variant
(intron variant)
Diabetes mellitus type 2, susceptibility to
Grisk factor
AGRP, ATP6V0D1-DT
(A67T)
Single nucleotide variant
(missense variant)
Inherited obesity
GBenign
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